FDA Adverse Event
Malfunction
Summary report: N
8024190
MDR report key: 8024190
·
Received October 31, 2018
Report
- Report Number
- 8024190
- Event Type
- Malfunction
- Date Received
- October 31, 2018
- Date of Event
- October 22, 2018
- Report Date
- October 26, 2018
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- FL
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
SKIN PEELING WAS NOTED ON LEFT MEDIAL THIGH WHEN THE DRAPES/IOBAN WAS PULLED OFF. SKIN TEAR NOTED ON THE RIGHT SCAPULA FROM THE R2 PAD SITE WHEN PADS WERE TAKEN OFF. MANUFACTURER'S GUIDELINES WERE FOLLOWED WHEN TAKING OFF R2 PADS. THERE WAS SLOUGHING OF SKIN ON LEFT INNER THIGH WITH REGARD DEFIBRILLATOR PADS.
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 25185 DA | Other |